EP0404175B1 - Procédé pour la préparation de dérivés d'imidazole - Google Patents

Procédé pour la préparation de dérivés d'imidazole Download PDF

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Publication number
EP0404175B1
EP0404175B1 EP90111875A EP90111875A EP0404175B1 EP 0404175 B1 EP0404175 B1 EP 0404175B1 EP 90111875 A EP90111875 A EP 90111875A EP 90111875 A EP90111875 A EP 90111875A EP 0404175 B1 EP0404175 B1 EP 0404175B1
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EP
European Patent Office
Prior art keywords
nitrite
imidazole derivatives
general formula
mol
mmol
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
EP90111875A
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German (de)
English (en)
Other versions
EP0404175A1 (fr
Inventor
Aiichiro C/O Mitsui Petrochemical Ind. Ltd. Ori
Junichi C/O Mitsui Petrochemical Ind. Ltd Imuta
Noriaki C/O Mitsui Petrochemical Ind. Ltd Kihara
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Mitsui Petrochemical Industries Ltd
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Mitsui Petrochemical Industries Ltd
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Publication date
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Priority to AT9090111875T priority Critical patent/ATE104975T1/de
Publication of EP0404175A1 publication Critical patent/EP0404175A1/fr
Application granted granted Critical
Publication of EP0404175B1 publication Critical patent/EP0404175B1/fr
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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00—Drugs for disorders of the senses
    • A61P27/02—Ophthalmic agents
    • A61P27/06—Antiglaucoma agents or miotics

Definitions

  • the present invention relates to an industrially advantageous process for preparing imidazole derivatives of the general formula (II): wherein R1 and R2 independently are C1-C4 alkyl. These compounds are useful for the treatment of glaucoma.
  • imidazole derivatives (II) from mercaptoimidazole derivatives (I) by desulfurization has also been known, for example, using Raney nickel in methoxyethanol [Tetrahedron, 28 , 967(1972)] or using hydrogen peroxide [J. Pharmaceutical Sciences, 64 , 1700(1975)].
  • the object of the present invention is to provide an industrially advantageous process for preparing imidazole derivatives (II) in high yield without the formation of the by-product isomer by desulfurizing the mercaptoimidazole derivative (I), wherein said desulfurization is carried out using inexpensive reagent.
  • the inventors have surprisingly found that the imidazole derivatives (II) can be obtained in extremely high yield and substantially without the formation of the by-product, by utilizing inexpensive nitric acid and a nitrite as desulfurizing agent.
  • the present invention relates to a process for preparing imidazole derivatives of the general formula (II): wherein R1 and R2 independently are C1-C4 alkyl, which comprises desulfurizing a mercaptoimidazole derivative of the general formula (I): wherein R1 and R2 are as defined above, with 1 to 50 mol per mol of I of nitric acid in the presence of 0.1 to 10 mol of a nitrite.
  • the mercaptoimidazole derivatives (I) used as a starting material in the present invention are publicly known and can be prepared, for example, according to the method described in Tetrahedron, 28 , 967(1972).
  • the desulfurization of the present invention may be conducted by contacting the starting material (I) with nitric acid in the presence of a nitrite without solvent or in an inert solvent such as water, ethanol, methyl cellosolve, dimethoxyethane, dioxane or acetic acid.
  • a nitrite without solvent or in an inert solvent such as water, ethanol, methyl cellosolve, dimethoxyethane, dioxane or acetic acid.
  • nitrites which generate nitrite ion may be used as a nitrite in the process of the present invention.
  • Typical nitrites which may be mentioned include, for example, inorganic nitrites such as sodium nitrite, potassium nitrite, barium nitrite, etc., and organic nitrites such as dimethylammonium nitrite, dicyclohexylammonium nitrite.
  • the amount of nitric acid is in the range of 1 to 50 mol, preferably 2 to 20 mol per mol of the starting material mercaptoimidazole derivative (I), and the nitrite is 0.1 to 10 mol, preferably 0.2 to 5 mol.
  • the solvent is used in 2 to 100 times, preferably 5 to 30 times the weight of the starting material.
  • the reaction is performed at a temperature of -30°C to 100°C, preferably at 3°C to 50°C, for 1 minute to 10 hours, preferably 10 minutes to 5 hours.
  • the imidazole derivative (II) thus formed is isolated after conventional separation and purification.
  • R1 is ethyl and R2 is methyl
  • R1 and R2 individually are C1-C4 alkyl such as methyl, ethyl, propyl, butyl.
  • the reaction mixture was made alkaline by adding 0.5 ml of 35% aqueous ammonia and extracted with 5 ml of chloroform.
  • the chloroform extract was dried over anhydrous sodium sulfate and evaporated to give 69.3 mg(84%) of pilocarpine as white crystals.
  • the crystals were dissolved in ethanol, filtrated to remove insolubles, 0.1 ml of concentrated hydrochloric acid added, and evaporated to give 77 mg(79%) of white crystals having a m.p. of 200-203°C.
  • 1H-NMR and mass spectrum (molecular ion peak at 208) of the crystals thus obtained are identical with those of the authentic sample pilocarpine hydrochloride.
  • Example 1 The procedure of Example 1 was followed using 7 mg(0.10 mmol) of sodium nitrite instead of 42 mg(0.60 mmol). Yield of pilocarpine: 85%.
  • Example 1 The procedure of Example 1 was followed using 14 mg(0.20 mmol) of sodium nitrite instead of 42 mg(0.60 mmol). Yield of pilocarpine: 92%.
  • Example 1 The procedure of Example 1 was followed using 14 mg(0.20 mmol) of sodium nitrite instead of 42 mg(0.60 mmol), and the reaction was performed at 40°C. Yield of pilocarpine: 90%.
  • Example 1 The procedure of Example 1 was followed using 2.0 ml of acetic acid as a solvent instead of 2.0 ml of water without the presence of a nitrite. Yield of pilocarpine: 77%.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Ophthalmology & Optometry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Plural Heterocyclic Compounds (AREA)

Claims (1)

  1. Procédé de préparation de dérivés d'imidazole de formule générale (II) :
    Figure imgb0008
     dans laquelle R¹ et R² représentent indépendamment des groupes alkyle en C₁₋₄,
    qui comporte la désulfuration d'un dérivé de mercaptoimidazole de formule générale (I) :
    Figure imgb0009
     dans laquelle R¹ et R² sont tels que définis ci-dessus,
    à l'aide de 1 à 50 moles d'acide nitrique par mole de composé (I), et en présence de 0,1 à 10 moles d'un nitrite.
EP90111875A 1989-06-22 1990-06-22 Procédé pour la préparation de dérivés d'imidazole Expired - Lifetime EP0404175B1 (fr)

Priority Applications (1)

Application Number Priority Date Filing Date Title
AT9090111875T ATE104975T1 (de) 1989-06-22 1990-06-22 Verfahren zur herstellung von imidazol-derivaten.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP1158403A JP2771257B2 (ja) 1989-06-22 1989-06-22 イミダゾール誘導体の製法
JP158403/89 1989-06-22

Publications (2)

Publication Number Publication Date
EP0404175A1 EP0404175A1 (fr) 1990-12-27
EP0404175B1 true EP0404175B1 (fr) 1994-04-27

Family

ID=15670988

Family Applications (1)

Application Number Title Priority Date Filing Date
EP90111875A Expired - Lifetime EP0404175B1 (fr) 1989-06-22 1990-06-22 Procédé pour la préparation de dérivés d'imidazole

Country Status (7)

Country Link
EP (1) EP0404175B1 (fr)
JP (1) JP2771257B2 (fr)
KR (1) KR920004137B1 (fr)
AT (1) ATE104975T1 (fr)
CA (1) CA2018978C (fr)
DE (1) DE69008431T2 (fr)
HU (1) HU210053B (fr)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4033612A1 (de) * 1990-10-23 1992-04-30 Merck Patent Gmbh Verfahren zur herstellung von racemischen pilosinin-derivaten
RU2761436C1 (ru) 2017-11-17 2021-12-08 Целликс Био Прайвет Лимитед Композиции и способы лечения нарушений со стороны органа зрения

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
JOURNAL OF PHARMACEUTICAL SCIENCES, vol. 64, no. 10, October 1975, pages 1700-1701; J.I. DEGRAW et al.: "Synthesis of d-pilocarpine-N-14CH3" *
TETRAHEDRON, vol. 28, no. 4, February 1972, pages 967-972; J.I. DEGRAW: "An improved synthesis of pilocarpine" *

Also Published As

Publication number Publication date
ATE104975T1 (de) 1994-05-15
KR920004137B1 (ko) 1992-05-25
DE69008431D1 (de) 1994-06-01
EP0404175A1 (fr) 1990-12-27
HU903953D0 (en) 1990-11-28
JP2771257B2 (ja) 1998-07-02
KR910000712A (ko) 1991-01-30
CA2018978A1 (fr) 1990-12-22
HU210053B (en) 1995-01-30
CA2018978C (fr) 1997-02-25
JPH0324077A (ja) 1991-02-01
HUT58080A (en) 1992-01-28
DE69008431T2 (de) 1994-09-29

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